Charles River Laboratories Jul 2016 - Jul 2017
Research Director Discovery Services
Charles River Laboratories Jul 2016 - Jul 2017
Senior Research Director
Unc Lineberger Comprehensive Cancer Center Feb 2016 - Jun 2016
Senior Associate of Drug Development
Meryx Apr 2015 - Feb 2016
Head of Biology
Gsk Sep 2013 - Mar 2015
Director of Biological Sciences
Education:
The Johns Hopkins University School of Medicine 1990 - 1991
University of North Carolina at Chapel Hill 1984 - 1989
Doctorates, Doctor of Philosophy, Biology
University of North Carolina at Chapel Hill 1980 - 1984
Bachelors, Bachelor of Science, Zoology
Skills:
Drug Discovery Assay Development Biochemistry Molecular Biology Cell Biology Biotechnology Cancer Genetics High Throughput Screening Biophysics Lead Change Target Identification Enzymes Lifesciences Laboratory Automation Enzymology Group Leadership Drug Discovery Project Leadership Protein Biochemistry
Edgar Wood (18601935) was an architect who practised from Manchester about the turn of the century and gained a considerable reputation both in Britain ...
Philip Harris - Durham NC, US Robert McNutt - Durham NC, US Lee Kuyper - Durham NC, US Karen Lackey - Durham NC, US Michael Peel - Durham NC, US Edgar Wood - Durham NC, US
International Classification:
A61K031/53 A61K031/454 A61K031/4196 A61K031/405 C 07D 4 3/02 C07D487/02
The present invention is related to oxindole derivatives, compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen activated signaling pathways in general, and in particular in the inhibition or antagonism of protein kinases, which pathologically involve aberrant cellular proliferation. Such disease states include tumor growth, restenosis, atherosclerosis, pain and thrombosis. In particular, the present invention relates to a series of substituted oxindole compounds, which exhibit Trk family protein tyrosine kinase inhibition, and which are useful in cancer therapy and chronic pain indications.
Karen Lackey - Durham NC, US Edgar Wood - Durham NC, US
International Classification:
C07D471/02 A61K031/4745
US Classification:
514/300000, 546/113000
Abstract:
The present invention is related to aza-oxindole derivatives formula (I), wherein X is N and Z is CHo; X is CH and Z is N, compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen activated signaling pathways in general, and in particular in the inhibition or antagonism of protein kinases, which pathologically involve aberrant cellular proliferation. Such disease states include tumor growth, restenosis, atherosclerosis, pain and thrombosis. In particular, the present invention relates to a series of substituted oxindole compounds, which exhibit Trk family protein tyrosine kinase inhibition, and which are useful in cancer therapy and chronic pain indications.
Substituted Oxindole Derivatives As Tyrosine Kinase Inhibitors
Scott Dickerson - Durham NC, US Robert Hunter - Durham NC, US Lee Kuyper - Durham NC, US Karen Lackey - Durham NC, US Michael Luzzio - Noank CT, US Edgar Wood - Durham NC, US
The present invention is related to oxindole derivatives of structure (I), compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen activated signaling pathways in general, and in particular in the inhibition or antagonism of protein kinases, which pathologically involve aberrant cellular proliferation. Such disease states include tumor growth, restenosis, atherosclerosis, pain and thrombosis. In particular, the present invention relates to a series of substituted oxindole compounds, which exhibit Trk family protein tyrosine kinase inhibition, and which are useful in cancer therapy and chronic pain indications.
Philip Harris - Durham NC, US Robert Hunter - Durham NC, US Lee Kuyper - Durham NC, US Karen Lackey - Durham NC, US Robert McNutt - Durham NC, US Michael Peel - Durham NC, US Edgar Wood - Durham NC, US
The present invention is related to oxindole derivatives, compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen activated signaling pathways in general, and in particular in the inhibition or antagonism of protein kinases, which pathologically involve aberrant cellular proliferation. Such disease states include tumor growth, restenosis, atherosclerosis, pain and thrombosis. In particular, the present invention relates to a series of substituted oxindole compounds, which exhibit Trk family protein tyrosine kinase inhibition, and which are useful in cancer therapy and chronic pain indications.
Karen Lackey - Durham NC, US Edgar Wood - Durham NC, US
International Classification:
A61K 31/4745 C07D 471/02
US Classification:
514300000, 546113000
Abstract:
The present invention is related to aza-oxindole derivatives, compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen activated signaling pathways in general, and in particular in the inhibition or antagonism of protein kinases, which pathologically involve aberrant cellular proliferation. Such disease states include tumor growth, restenosis, atherosclerosis, pain and thrombosis. In particular, the present invention relates to a series of substituted oxindole compounds, which exhibit Trk family protein tyrosine kinase inhibition, and which are useful in cancer therapy and chronic pain indications.
Karen LACKEY - Durham NC, US Robert Mullen - Durham NC, US Neil Spector - Chapel Hill NC, US Edgar Wood - Durham NC, US Wenie Xia - Durham NC, US
International Classification:
A61K 33/24 A61K 31/517 A61K 31/282
US Classification:
424649000, 514266240, 514492000
Abstract:
A method of treating cancer is described including administration of a 4-quinazolineamine and at least one other anti-neoplastic agent as well as a pharmaceutical combination including the 4-quinazolineamines.
San DiegoPast: Travel Consultant at Plaza Travel I'm a Travel Agent working out of my home in San Diego, CA. I specialize in Cruises, European River Crusies, Tours and All inclusive Resorts. I have been a... I'm a Travel Agent working out of my home in San Diego, CA. I specialize in Cruises, European River Crusies, Tours and All inclusive Resorts. I have been a travel agent for 22yrs. and have clients thoughout the US.